Fig. 6From: Insights from molecular docking and molecular dynamics on the potential of vitexin as an antagonist candidate against lipopolysaccharide (LPS) for microglial activation in neuroinflammationAnalysis of (A) residue-wise RMSF and (B) protein secondary structure elements (SSE) of TLR4/MD-2 complex upon binding with vitexin. The red columns indicate alpha helices whereby blue columns indicate beta-strandsBack to article page